Publicaciones en las que colabora con ÁLVARO GALLEGO MARTÍNEZ (8)

2022

  1. A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss

    European Journal of Human Genetics, Vol. 30, Núm. 11, pp. 1301-1305

  2. Defective α‐tectorin may involve tectorial membrane in familial Meniere disease

    Clinical and Translational Medicine

  3. Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitus

    npj Genomic Medicine, Vol. 7, Núm. 1

2020

  1. Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease

    Ear and Hearing, Vol. 41, Núm. 6, pp. 1598-1605

  2. Clinical and molecular genetics of Meniere disease

    Medizinische Genetik, Vol. 32, Núm. 2, pp. 141-148

  3. Enrichment of damaging missense variants in genes related with axonal guidance signalling in sporadic Meniere's disease

    Journal of Medical Genetics, Vol. 57, Núm. 2, pp. 82-88

2019

  1. Excess of Rare Missence Variants in Hearing Loss Genes in Sporadic Meniere Disease

    Frontiers in Genetics, Vol. 10, Núm. FEB

2018

  1. Genetics of vestibular syndromes

    Current Opinion in Neurology, Vol. 31, Núm. 1, pp. 105-110